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111.
The co-extraction phenomenon was found in a typical chelate extraction system, in which the extraction of lanthanoid ion (Ln3+) with acetylacetone (Hacac) was highly enhanced by various metal ions (M(n+)) such as Cu2+, Al3+, and Zr4+. This phenomenon was ascribed to the formation of the 1:1 adduct between Ln(acac)3 and the M(acac),, extracted into the organic phase. The co-extraction occurred more readily for La3+ than that for Lu3+, and increased in the order of Cu2+ < Al3+ < Zr4+. This work elucidated that the co-extraction due to the adduct formation is a rather common phenomenon in the chelate extraction. 相似文献
112.
M. Hoshino M. Takai K. Fukuda K. Imura J. Hayashi 《Journal of polymer science. Part A, Polymer chemistry》1989,27(6):2083-2092
The application of NMR for natural organic compounds has been carried out from the early history of NMR. But they reported on the liquid state NMR and the samples were limited to the materials which dissolved in proper solvents. It has been possible to measure the samples in the solid state in 1970s and is widely used as a familiar analytical method in 1980s. Whereas some of the data is inadequate, concerning cellulose derivatives, in particular, only nitrate and acetate were reported by Patterson1 and Doyle,2 respectively. In this paper, the 13C CP/MAS solid state NMR spectra of several cellulose derivatives are shown and the relationship between the structure and spectrum is discussed. 相似文献
113.
Katsuhiko Ono Shoji Tanaka Yoshiro Yamashita 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》1994,106(19):2030-2032
114.
This paper considers the set packing problem max{wx: Ax b, x 0 and integral}, whereA is anm × n 0–1 matrix,w is a 1 ×n weight vector of real numbers andb is anm × 1 vector of ones. In equality form, its linear programming relaxation is max{wx: (x, y) P(A)} whereP(A) = {(x, y):Ax +I
m
y =b, x0,y0}. Letx
1 be any feasible solution to the set packing problem that is not optimal and lety
1 =b – Ax
1; then (x
1,y
1) is an integral extreme point ofP(A). We show that there exists a sequence of simplex pivots from (x
1,y
1) to (x*,y*), wherex* is an optimal solution to the set packing problem andy* =b – Ax*, that satisfies the following properties. Each pivot column has positive reduced weight and each pivot element equals plus one. The number of pivots equals the number of components ofx* that are nonbasic in (x
1,y
1).This research was supported by NSF Grants ECS-8005360 and ECS-8307473 to Cornell University. 相似文献
115.
N. Suzuki A. Nakadate H. Imura 《Journal of Radioanalytical and Nuclear Chemistry》1991,149(1):149-159
The synergic extraction of La(III), Eu(III), and Lu(III) with 2-thenoyltrifluoroacetone (Htta) and triphenylarsine oxide (tpao) in benzene has been studied. The extractability of lanthanoids, Ln(III), is significantly affected by the association of Htta with tpao in the organic phase. The associated species is Htta·tpao and the association constant is determined as 101.63. The intrinsic extraction equilibrium of Ln(III) is analyzed using the free concentration of Htta and tpao. The synergic enhancement is ascribable to the formation of the adduct complexes shown as Ln(tta)3tpao and Ln(tta)3(tpao)2 in the present extraction system. The adduct formation constants determined are very large as expected from the high basicity of tpao. 相似文献
116.
The extraction of La(III), Gd(III), and Lu(III) with 18-crown-6 (18C6) has been studied using pentadecafluorooctanoate (PDFO) as a counter anion. Very high extractability of La(III) was observed in various organic solvents such as benzene, chloroform, 1,2-dichloroethane, and nitrobenzene. The predominant species extracted into benzene was found to be Ln(PDFO)3 (18C6), and the extraction constants (K
ex,s1
=[Ln(PDFO)3 (18C6)]org/[Ln3+][PDFO]3[18C6]org) were 1013.12 for La(III), 109.74 for Gd(III), and 109.67 for Lu(III). These values are 1010 times higher than those in the trichloroacetate-18C6 system reported previously. The present PDFO-18C6 system was superior to the picrate- and hexafluoroacetylacetonate-18C6 system for the separation efficiency of light lanthanides(III). 相似文献
117.
Kunio Mori Yoshiro Nakamura 《Journal of polymer science. Part A, Polymer chemistry》1978,16(8):2055-2062
Crosslinking of poly(vinyl chloride) (PVC) with 2-R-4,6-dithiol-s-triazine (R-DT) and metal activators has been studied to determine crosslinking rate constants, induction periods, and apparent activation energy and the final efficiency of crosslinking agents. The rate constants were about 1.4–7.5 min?1 and the induction periods were about 6.8–24.3 min for various kinds of R-DT at 180°C. The activation energy was about 16.6–33 kcal/mol over the temperature range 160–195°C. The rate constants were strongly influenced by 2-substituted groups (R) in R-DT and increased in the order R′O-? R′NH-< (R′)2N, where R′ is an alkyl or aryl group. Further, the rate constants increased in the order of: metal carboxylates < metal carboxylates < metal oxides for the activators and in the order of: Pb < Mg < Ca < Ba < Na for metal atoms. The final efficiency was about 75–80% for the activators such as MgO, MgCO3, PbO, and SnO. The activators containing Na, Ca, and Ba atoms, however, gave final efficiency of more than 100%. 相似文献
118.
Jun-Ichi Matsumoto Teruyuki Miyamoto Akira Minamida Yoshiro Nishimura Hiroshi Egawa Haruki Nishimura 《Journal of heterocyclic chemistry》1984,21(3):673-679
Fluorination of the 2,6-disubstituted 3-aminopyridines 5 and 12 by the Balz-Schiemann reaction is described. 2,6-Dichloro-3-pyridinediazonium tetrafluoroborate ( 6 ) and 2-substituted 6-acetylamino-3-pyridinediazonium tetrafluoroborates 13 were heated with or without a solvent to give the corresponding fluorinated pyridines 7 and 14 , respectively, in good yields. 2-Substituted 6-acetylamino-3-fluoropyridines ( 14 ) were converted by a known method into a series of 7-substituted 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids 21 including enoxacin [1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic acid [( 2 )], a new potential antibacterial agent. 相似文献
119.
The substoichiometric isotope dilution analysis for U(VI) in a synergic extraction system of an excess amount of a chelating agent HHFA and a substoichiometric amount of neutral ligand TOPO has been developed. A constant but substoichiometric amout of U(VI) can be precisely extracted, and U down to ppm levels can be accurately determined by the present method. This method was applied to the analysis of a phosphate rock. 相似文献
120.
Yoshiro Ito Hajime Ohtani Shouji Ueda Yasuki Nakashima Shin Tsuge 《Journal of polymer science. Part A, Polymer chemistry》1994,32(2):383-388
The determination of end groups in polystyrenes (PSts) polymerized anionically with n-butyllithium as the initiator was carried out by pyrolysis-gas chromatography (Py-GC). The relative proportions of the end groups decrease with increasing molecular weight (MW). Consequently, the peaks which reflect the structure of the end groups can be distinguished by comparing pyrograms of samples with different MW. By comparing the intensities of these peaks relative to total intensities of all the peaks in the pyrogram, the numberaverage molecular weight (Mn) of the polymer can be estimated. The observed Mn values of PSts estimated by this method are compared with those determined by size exclusion chromatography (SEC). By this method it was possible to make direct determination of Mn values of PSts with MWs between 1000 and ca. 1 million. Furthermore, the calibration curve produced by the relative intensity of one of the most characteristic peaks (2-phenyl-1-heptene; C4H9? CH2C (Ph) = CH2) for the end group to total intensity of all the peaks in the pyrogram, gave rapid and highly reproducible Mn values. © 1994 John Wiley & Sons, Inc. 相似文献